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Gynetech Pty. , Ltd.

4 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
ManipulatOR PRO, ManipulatOR (K150519)Gynetech Pty. , Ltd.2015-08-19
InsufflatOR Needle (K142700)Gynetech Pty. , Ltd.2014-12-19
MANIPULATOR; MANIPULATOR PRO (K142164)Gynetech Pty. , Ltd.2014-12-17
MCCARTNEY ACCESS TUBE (K051594)Gynetech Pty. , Ltd.2005-09-02

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Every clearance here is in the API, with alerts when new ones post.